Canonical Allele Identifier: CA2201991753
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2049081_2049085delinsGTTCT , CM000678.2:g.2049081_2049085delinsGTTCT GRCh38
NC_000016.9:g.2099082_2099086delinsGTTCT , CM000678.1:g.2099082_2099086delinsGTTCT GRCh37
NC_000016.8:g.2039083_2039087delinsGTTCT NCBI36
NG_005895.1:g.4776_4780delinsGTTCT , LRG_487:g.4776_4780delinsGTTCT
NG_008412.1:g.3782_3786delinsAGAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.138+328_138+332delinsGTTCT ENSP00000455997.2:n.138+328_138+332delinsGTTCT
ENST00000642206.2:c.138+328_138+332delinsGTTCT ENSP00000495146.2:n.138+328_138+332delinsGTTCT
ENST00000642365.2:c.138+328_138+332delinsGTTCT ENSP00000495459.2:n.138+328_138+332delinsGTTCT
ENST00000644417.2:c.138+328_138+332delinsGTTCT ENSP00000493912.2:n.138+328_138+332delinsGTTCT
ENST00000646464.2:c.138+328_138+332delinsGTTCT ENSP00000496610.2:n.138+328_138+332delinsGTTCT
ENST00000219476.9:c.138+328_138+332delinsGTTCT MANE Select ENSP00000219476.3:n.138+328_138+332delinsGTTCT
ENST00000350773.9:c.138+328_138+332delinsGTTCT ENSP00000344383.4:n.138+328_138+332delinsGTTCT
ENST00000401874.7:c.138+328_138+332delinsGTTCT ENSP00000384468.2:n.138+328_138+332delinsGTTCT
ENST00000461648.3:n.248+328_248+332delinsGTTCT
ENST00000568454.6:c.171+328_171+332delinsGTTCT ENSP00000454487.1:n.171+328_171+332delinsGTTCT
ENST00000568692.2:n.18+328_18+332delinsGTTCT
ENST00000642206.1:c.138+328_138+332delinsGTTCT ENSP00000495146.1:n.138+328_138+332delinsGTTCT
ENST00000642561.1:c.138+328_138+332delinsGTTCT ENSP00000495099.1:n.138+328_138+332delinsGTTCT
ENST00000642797.1:c.138+328_138+332delinsGTTCT ENSP00000493846.1:n.138+328_138+332delinsGTTCT
ENST00000642812.1:n.195+328_195+332delinsGTTCT
ENST00000642936.1:c.138+328_138+332delinsGTTCT ENSP00000494514.1:n.138+328_138+332delinsGTTCT
ENST00000643088.1:c.138+328_138+332delinsGTTCT ENSP00000494747.1:n.138+328_138+332delinsGTTCT
ENST00000643149.1:n.248+328_248+332delinsGTTCT
ENST00000643298.1:c.138+328_138+332delinsGTTCT ENSP00000494393.1:n.138+328_138+332delinsGTTCT
ENST00000643745.1:c.138+328_138+332delinsGTTCT ENSP00000495948.1:n.138+328_138+332delinsGTTCT
ENST00000643946.1:c.138+328_138+332delinsGTTCT ENSP00000495927.1:n.138+328_138+332delinsGTTCT
ENST00000644043.1:c.138+328_138+332delinsGTTCT ENSP00000496262.1:n.138+328_138+332delinsGTTCT
ENST00000644135.1:c.138+328_138+332delinsGTTCT ENSP00000495644.1:n.138+328_138+332delinsGTTCT
ENST00000644222.1:n.225+328_225+332delinsGTTCT
ENST00000644329.1:c.138+328_138+332delinsGTTCT ENSP00000496611.1:n.138+328_138+332delinsGTTCT
ENST00000644335.1:c.138+328_138+332delinsGTTCT ENSP00000496317.1:n.138+328_138+332delinsGTTCT
ENST00000644399.1:c.131+328_131+332delinsGTTCT
ENST00000644665.1:n.255+328_255+332delinsGTTCT
ENST00000645591.1:n.266+328_266+332delinsGTTCT
ENST00000646388.1:c.138+328_138+332delinsGTTCT ENSP00000495921.1:n.138+328_138+332delinsGTTCT
ENST00000647234.1:n.13+328_13+332delinsGTTCT
ENST00000219476.7:c.138+328_138+332delinsGTTCT ENSP00000219476.3:n.138+328_138+332delinsGTTCT
ENST00000350773.8:c.138+328_138+332delinsGTTCT ENSP00000344383.4:n.138+328_138+332delinsGTTCT
ENST00000382538.10:c.-10+1016_-10+1020delinsGTTCT ENSP00000371978.6:n.-10+1016_-10+1020delinsGTTCT
ENST00000401874.6:c.138+328_138+332delinsGTTCT ENSP00000384468.2:n.138+328_138+332delinsGTTCT
ENST00000439117.6:c.138+328_138+332delinsGTTCT ENSP00000406980.2:n.138+328_138+332delinsGTTCT
ENST00000439673.6:c.138+328_138+332delinsGTTCT ENSP00000399232.2:n.138+328_138+332delinsGTTCT
ENST00000461648.2:n.243+328_243+332delinsGTTCT
ENST00000568454.5:c.171+328_171+332delinsGTTCT ENSP00000454487.1:n.171+328_171+332delinsGTTCT
NM_000548.3:c.138+328_138+332delinsGTTCT , LRG_487t1:c.138+328_138+332delinsGTTCT NP_000539.2:n.138+328_138+332delinsGTTCT
NM_001077183.1:c.138+328_138+332delinsGTTCT NP_001070651.1:n.138+328_138+332delinsGTTCT
NM_001114382.1:c.138+328_138+332delinsGTTCT NP_001107854.1:n.138+328_138+332delinsGTTCT
XM_005255529.3:c.138+328_138+332delinsGTTCT XP_005255586.2:n.138+328_138+332delinsGTTCT
XM_005255531.3:c.138+328_138+332delinsGTTCT XP_005255588.2:n.138+328_138+332delinsGTTCT
XM_011522636.1:c.138+328_138+332delinsGTTCT XP_011520938.1:n.138+328_138+332delinsGTTCT
XM_011522637.1:c.138+328_138+332delinsGTTCT XP_011520939.1:n.138+328_138+332delinsGTTCT
XM_011522638.1:c.138+328_138+332delinsGTTCT XP_011520940.1:n.138+328_138+332delinsGTTCT
XM_011522639.1:c.138+328_138+332delinsGTTCT XP_011520941.1:n.138+328_138+332delinsGTTCT
XM_011522640.1:c.138+328_138+332delinsGTTCT XP_011520942.1:n.138+328_138+332delinsGTTCT
XM_011522641.1:c.138+328_138+332delinsGTTCT XP_011520943.1:n.138+328_138+332delinsGTTCT
NM_000548.4:c.138+328_138+332delinsGTTCT NP_000539.2:n.138+328_138+332delinsGTTCT
NM_001077183.2:c.138+328_138+332delinsGTTCT NP_001070651.1:n.138+328_138+332delinsGTTCT
NM_001114382.2:c.138+328_138+332delinsGTTCT NP_001107854.1:n.138+328_138+332delinsGTTCT
NM_001318827.1:c.138+328_138+332delinsGTTCT NP_001305756.1:n.138+328_138+332delinsGTTCT
NM_001318829.1:c.-10+1016_-10+1020delinsGTTCT NP_001305758.1:n.-10+1016_-10+1020delinsGTTCT
NM_001318831.1:c.-89+328_-89+332delinsGTTCT NP_001305760.1:n.-89+328_-89+332delinsGTTCT
NM_001318832.1:c.171+328_171+332delinsGTTCT NP_001305761.1:n.171+328_171+332delinsGTTCT
NM_001363528.1:c.138+328_138+332delinsGTTCT NP_001350457.1:n.138+328_138+332delinsGTTCT
NM_021055.2:c.138+328_138+332delinsGTTCT NP_066399.2:n.138+328_138+332delinsGTTCT
XM_005255531.4:c.138+328_138+332delinsGTTCT XP_005255588.2:n.138+328_138+332delinsGTTCT
XM_011522636.2:c.138+328_138+332delinsGTTCT XP_011520938.1:n.138+328_138+332delinsGTTCT
XM_011522637.2:c.138+328_138+332delinsGTTCT XP_011520939.1:n.138+328_138+332delinsGTTCT
XM_011522638.2:c.411+328_411+332delinsGTTCT XP_011520940.2:n.411+328_411+332delinsGTTCT
XM_011522639.2:c.138+328_138+332delinsGTTCT XP_011520941.1:n.138+328_138+332delinsGTTCT
XM_011522640.2:c.138+328_138+332delinsGTTCT XP_011520942.1:n.138+328_138+332delinsGTTCT
XM_017023615.1:c.138+328_138+332delinsGTTCT XP_016879104.1:n.138+328_138+332delinsGTTCT
XM_017023616.1:c.138+328_138+332delinsGTTCT XP_016879105.1:n.138+328_138+332delinsGTTCT
XM_017023617.1:c.411+328_411+332delinsGTTCT XP_016879106.1:n.411+328_411+332delinsGTTCT
XM_017023618.1:c.-1294+328_-1294+332delinsGTTCT XP_016879107.1:n.-1294+328_-1294+332delinsGTTCT
XM_024450413.1:c.138+328_138+332delinsGTTCT XP_024306181.1:n.138+328_138+332delinsGTTCT
NM_000548.5:c.138+328_138+332delinsGTTCT MANE Select NP_000539.2:n.138+328_138+332delinsGTTCT
NM_001370404.1:c.138+328_138+332delinsGTTCT NP_001357333.1:n.138+328_138+332delinsGTTCT
NM_001370405.1:c.138+328_138+332delinsGTTCT NP_001357334.1:n.138+328_138+332delinsGTTCT
NM_001077183.3:c.138+328_138+332delinsGTTCT NP_001070651.1:n.138+328_138+332delinsGTTCT
NM_001114382.3:c.138+328_138+332delinsGTTCT NP_001107854.1:n.138+328_138+332delinsGTTCT
NM_001318827.2:c.138+328_138+332delinsGTTCT NP_001305756.1:n.138+328_138+332delinsGTTCT
NM_001318829.2:c.-10+1016_-10+1020delinsGTTCT NP_001305758.1:n.-10+1016_-10+1020delinsGTTCT
NM_001318831.2:c.-89+328_-89+332delinsGTTCT NP_001305760.1:n.-89+328_-89+332delinsGTTCT
NM_001318832.2:c.171+328_171+332delinsGTTCT NP_001305761.1:n.171+328_171+332delinsGTTCT
NM_001363528.2:c.138+328_138+332delinsGTTCT NP_001350457.1:n.138+328_138+332delinsGTTCT
NM_021055.3:c.138+328_138+332delinsGTTCT NP_066399.2:n.138+328_138+332delinsGTTCT